Your session is about to expire
← Back to Search
Other
MET642 for Non-alcoholic Fatty Liver Disease
Phase 2
Waitlist Available
Research Sponsored by Metacrine, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 28 days after last dose
Awards & highlights
Study Summary
This study is evaluating whether a drug called MET642 can improve liver function in people with nonalcoholic steatohepatitis (NASH).
Eligible Conditions
- Non-alcoholic Fatty Liver Disease
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 28 days after last dose
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 28 days after last dose
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Adverse Events
ECG
Laboratory tests
+1 moreSecondary outcome measures
Pharmacodynamic Profile of MET642
Pharmacokinetic Profile of MET642
Pharmacological Activity of MET642
Trial Design
3Treatment groups
Experimental Treatment
Placebo Group
Group I: MET642 low doseExperimental Treatment1 Intervention
Group II: MET642 high doseExperimental Treatment1 Intervention
Group III: MET642 PlaceboPlacebo Group1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
MET642
2021
Completed Phase 2
~220
Find a Location
Who is running the clinical trial?
Metacrine, Inc.Lead Sponsor
1 Previous Clinical Trials
120 Total Patients Enrolled
1 Trials studying Non-alcoholic Fatty Liver Disease
120 Patients Enrolled for Non-alcoholic Fatty Liver Disease
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Share this study with friends
Copy Link
Messenger